A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv771175



Internal ID16065131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:40832545..41463140hg38UCSC Ensembl
Innerchr11:40854095..41484690hg19UCSC Ensembl
Innerchr11:40810671..41441266hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38630596
hg19630596
hg18630596
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv554093
Supporting Variants
Samples
Known GenesLRRC4C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv771175
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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